RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.): Medical Device Recall in 2016 - (Recall #: Z-1829-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve. Spinal fixation device instrument.

Product Classification:

Class II

Date Initiated: April 22, 2016

Date Posted: June 1, 2016

Recall Number: Z-1829-2016

Event ID: 74031

Reason for Recall:

Potential for a product defect where the cannula may be obstructed. This obstruction could prevent a driver from going through, which increases the potential for the driver to slip, resulting in possible patient injury.

Status: Terminated

Product Quantity: 17 devices

Code Information:

Streamline OCT Occipito-Cervico-Thoracic System, Crosslink Counter Torque Sleeve; Lot Number: 170684; Part Number: 26-COUNTER-T-XLINK

Distribution Pattern:

US nationwide distribution in CA, FL, IN, MI, MO, NC, NY, and TX.

Voluntary or Mandated:

Voluntary: Firm initiated